Senior Clinical Research Associate II – Oncology

Posted 21hrs ago

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Job Description

Oncology Sr. CRA 2 responsible for all aspects of study site monitoring. Ensuring adherence to protocols and maintaining integrity of trial data with considerable travel involved.

Responsibilities:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites
  • Conduct pre-study and initiation visits
  • Ensure study staff have proper materials and instructions
  • Verify informed consent procedures and protocol adherence
  • Monitor data for missing or implausible data

Requirements:

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 5+ years of Clinical Monitoring experience
  • Oncology experience, early phase preferred
  • 30-50% overnight travel

Benefits:

  • Health insurance
  • 401(k)
  • Paid time off
  • Remote work options
  • Professional development